HGVS | Genome Assembly |
---|---|
NC_000024.10:g.20579688C>G , CM000686.2:g.20579688C>G | GRCh38 |
NC_000024.9:g.22741574C>G , CM000686.1:g.22741574C>G | GRCh37 |
NC_000024.8:g.21150962C>G | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000361365.7:c.97C>G MANE Select | ENSP00000354722.2:p.Gln33Glu | |
ENST00000361365.6:c.97C>G | ENSP00000354722.2:p.Gln33Glu | |
ENST00000382772.3:c.97C>G | ENSP00000372222.3:p.Gln33Glu | |
ENST00000465253.1:n.191C>G | ||
NM_001278612.1:c.97C>G | NP_001265541.1:p.Gln33Glu | |
NM_004681.3:c.97C>G | NP_004672.2:p.Gln33Glu | |
NM_004681.4:c.97C>G MANE Select | NP_004672.2:p.Gln33Glu | |
NM_001278612.2:c.97C>G | NP_001265541.1:p.Gln33Glu |